Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

Aryldiazonium Salts to Azo Dyes: Diazo Coupling

3.8K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
3.8K
Cycloaddition Reactions: MO Requirements for Thermal Activation01:16

Cycloaddition Reactions: MO Requirements for Thermal Activation

5.0K
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
5.0K
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

3.1K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
3.1K
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

1.5K
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
1.5K
Aromatic Hydrocarbon Cations: Structural Overview01:18

Aromatic Hydrocarbon Cations: Structural Overview

4.2K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
4.2K
Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

2.4K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
2.4K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Large Magnetoresistance in a Si-Based Double-Tunnel Junction with Purely Organic Radical Molecules.

Nano letters·2026
Same author

Captodative Radicals Enable the Coexistence of Monomer and Dimer Single-Molecule Junctions with 100-Fold Difference in Conductance.

Journal of the American Chemical Society·2026
Same author

Acid-Catalyzed Rearrangement Reaction for Single-Molecule Junction Formation.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026
Same author

Mixed-Isomers Strategy for Thermally Stable and High-Performance Thick-Film All-Small-Molecule Organic Solar Cells.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

Carrier-Regulation in Organic Cathodes for Photochargeable Batteries Boosting High Photoresponse and Long Durability.

Nano letters·2026
Same author

A Highly Adhesive Binder Enables Sulfide-Based All-Solid-State Batteries with High Cycling Stability at Low Stack Pressure.

Small (Weinheim an der Bergstrasse, Germany)·2026
Same journal

Radical Cascades on Seawater Microdroplets Drive Atmospheric Mercury Oxidation.

Journal of the American Chemical Society·2026
Same journal

Superior Selective and Fast NH<sub>3</sub> Adsorption of Soft Porous MOF/Ionic Liquid Composites with Ordering Phase Transitions.

Journal of the American Chemical Society·2026
Same journal

Systematic Catalyst Variation for Improved Stereoselective Epoxide Polymerization: Subtle Modifications Resulting in Superior Efficiency.

Journal of the American Chemical Society·2026
Same journal

Deciphering the Halide Chemistry of Cl<sup>-</sup> and Br<sup>-</sup> in Enhancing Kinetics of Mg Plating/Stripping.

Journal of the American Chemical Society·2026
Same journal

Electrosynthesis of C<sub>6</sub> Chemicals by Propylene Oxidative Coupling on Au Surface.

Journal of the American Chemical Society·2026
Same journal

Statistical AI Enables Precise Screening of Multielement Catalysts.

Journal of the American Chemical Society·2026
See all related articles

Related Experiment Video

Updated: Mar 14, 2026

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
10:39

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction

Published on: August 23, 2018

8.4K

Host-Guest Interactions Enhance Charge Transport across Single Cyclodextrin/Azobenzene Complex Junction.

Song Han1, Jingjing Zhao2, Sumit Naskar3,4

  • 1Department of Physics, City University of Hong Kong, Kowloon, Hong Kong 999077, China.

Journal of the American Chemical Society
|March 12, 2026
PubMed
Summary
This summary is machine-generated.

Host-guest interactions between alpha-cyclodextrin (α-CD) and azobenzene influence single-molecule conductance. Complex formation enhances conductance, but this effect diminishes over time due to α-CD aggregation.

More Related Videos

Printing Fabrication of Bulk Heterojunction Solar Cells and In Situ Morphology Characterization
07:32

Printing Fabrication of Bulk Heterojunction Solar Cells and In Situ Morphology Characterization

Published on: January 29, 2017

11.7K
All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics
11:33

All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics

Published on: January 19, 2018

10.3K

Related Experiment Videos

Last Updated: Mar 14, 2026

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
10:39

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction

Published on: August 23, 2018

8.4K
Printing Fabrication of Bulk Heterojunction Solar Cells and In Situ Morphology Characterization
07:32

Printing Fabrication of Bulk Heterojunction Solar Cells and In Situ Morphology Characterization

Published on: January 29, 2017

11.7K
All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics
11:33

All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics

Published on: January 19, 2018

10.3K

Area of Science:

  • Molecular electronics
  • Supramolecular chemistry

Background:

  • Azobenzene's charge transport properties are well-studied.
  • The impact of host-guest complexation on azobenzene's molecular conductance is not well understood.

Purpose of the Study:

  • To investigate how host-guest interactions between alpha-cyclodextrin (α-CD) and azobenzene affect single-molecule conductance in aqueous solution.
  • To elucidate the role of molecular structure in modulating these effects.

Main Methods:

  • Experimental techniques: Nuclear Magnetic Resonance (NMR) and Ultraviolet-Visible (UV-Vis) spectroscopy to confirm host-guest complex formation.
  • Conductance measurements of amine-terminated azobenzene in aqueous solution with and without α-CD.
  • Comparison with modified molecules: amine-terminated stilbene and thiomethyl-terminated azobenzene.
  • Computational analysis: First-principles simulations to understand electronic structure changes.

Main Results:

  • Formation of an α-CD/azobenzene host-guest complex driven by azobenzene's hydrophobicity.
  • A ~3.5-fold increase in single-molecule conductance for amine-terminated azobenzene upon complexation.
  • Progressive attenuation of conductance enhancement over time, attributed to α-CD aggregation.
  • No significant conductance change observed for modified azobenzene or stilbene derivatives.

Conclusions:

  • Host-guest interactions significantly modulate single-molecule conductance of azobenzene.
  • The observed conductance enhancement is linked to the formation and stability of the α-CD/azobenzene complex.
  • Structural modifications influence the sensitivity of molecular conductance to host-guest interactions.
  • First-principles simulations support the experimental findings regarding electronic structure changes.